Status:

UNKNOWN

User Preference Study of an Experimental HydroGlyde Male Condom Compared to a Commercial Latex Male Condom

Lead Sponsor:

HydroGlyde Coatings, LLC

Collaborating Sponsors:

Essential Access Health

Conditions:

Condom Users

Eligibility:

All Genders

18-45 years

Phase:

EARLY_PHASE1

Brief Summary

Latex condoms have long been available as contraceptive devices as well as an effective means of preventing the spread of sexually transmitted infections. However, lack of adequate lubrication leads t...

Detailed Description

Latex condoms have long been available as contraceptive devices as well as an effective means of preventing the spread of sexually transmitted infections. However, lack of adequate lubrication leads t...

Eligibility Criteria

Inclusion

  • Between the ages of 18 and 45 years (inclusive)
  • Willing and able to give signed informed consent.
  • Willing to respond to questions concerning their reproductive and contraceptive history and use of condoms contained on self-administered questionnaires, online questionnaires or in-person interviews.
  • Have vaginal intercourse at least once weekly.
  • Protected against pregnancy by oral contraceptives, an intrauterine device, an implant, contraceptive injections, contraceptive patch, or sterilization (tubal ligation or vasectomy).
  • Willing to use the study products for four acts of vaginal intercourse within three weeks of study entry.
  • In a mutually monogamous relationship with their study partner for at least 6 months and be willing to remain mutually monogamous throughout study participation.
  • i. Agree not to wear any genital piercing jewelry or use sex toys while using the study condoms.
  • j. Agree not to use drugs that could enhance or diminish sexual response, including testosterone, poppers, and drugs like Viagra and Cialis when using study condoms.
  • k. Agree not to use alcohol in amounts that could enhance or diminish sexual response when using the condoms.
  • l. Agree to return any unopened condoms m. Have home access to the internet, a valid personal email for each partner and be reachable by mobile phone.
  • n. Willing to participate in either in-person visits or remote study visits conducted via videoconference and telephone and curbside exchange.
  • o. Agree to complete online questionnaires after testing each study product and group of study products.
  • p. Male partner agrees to ejaculate during vaginal intercourse. q. Willing to complete interviews by phone or video with HydroGlyde Coatings representatives.
  • r. Each partner has used 10 or more male condoms in their lifetime. s. Willing to sign a confidentiality agreement pertaining to the study condoms.

Exclusion

  • Currently participating in another clinical study.
  • Female partner self-reported as pregnant.
  • Allergic to natural rubber latex or has a history of recurrent adverse events following use of latex products.
  • Known allergy or skin sensitivity to common cosmetics and/or contact lens solutions or polyvinylpyrrolidone (PVP).
  • Unable to follow instructions or strictly adhere to the study schedule.
  • At significant (high) risk of sexually transmitted infections, including human immunodeficiency virus infection, or having a medical history of recurrent, serious sexually transmitted infection (e.g. gonorrhea, syphilis, chlamydia).
  • Currently using condoms for protection against a known sexually transmitted infection.
  • Taking any internally applied medication or oral medication to treat a genital condition.
  • Male partner has had difficulty achieving or maintaining an erection, or achieving ejaculation in the last month under typical circumstances/conditions.
  • Any self-reported genital condition (e.g. itching, burning, irritation, etc.) which, in the opinion of the investigator, could affect use of the study condoms or the ability to interpret study data.

Key Trial Info

Start Date :

March 1 2022

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

April 30 2022

Estimated Enrollment :

120 Patients enrolled

Trial Details

Trial ID

NCT05308992

Start Date

March 1 2022

End Date

April 30 2022

Last Update

April 4 2022

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Essential Access Health

Los Angeles, California, United States, 90010

User Preference Study of an Experimental HydroGlyde Male Condom Compared to a Commercial Latex Male Condom | DecenTrialz